Concepedia

Author

Kitiwan Rojnueangnit

Thammasat UniversityORCID

Also Known As

Gripp, Karen W., Hudson Freeze, K Rojnueangnit, Kitiwan Rojnueangnit

40

Publications

545

Citations

12

H-Index

52

Concepts

All Affiliations

Thammasat UniversityRamathibodi HospitalMahidol UniversityUniversity of Alabama at BirminghamThai Red Cross Society
KR

About

Kitiwan Rojnueangnit is an author at Thammasat University specializing in medicine, pediatrics, and child development.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

6

6

295

2

Engineering

1

1

15

3

Health Sciences

1

1

25

4

Language Studies

1

1

30

5

Natural Sciences

1

1

18

Kitiwan Rojnueangnit

×

13

Publications

464

Citations

12

H-Index

YearCitations

High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype–Phenotype Correlation

Kitiwan Rojnueangnit, Jing Xie, Alicia Gomes,

Human Mutation

2015

188

Oxygen saturation trends in preterm infants during the first 15 min after birth

Pracha Nuntnarumit, Kitiwan Rojnueangnit, Archara Tangnoo

Journal of Perinatology

2009

38

Hajdu–Cheney syndrome

Maria Descartes, Kitiwan Rojnueangnit, Laura E. Cole,

Clinical Dysmorphology

2014

30

Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder

Areerat Hnoonual, Weerin Thammachote, Thipwimol Tim‐Aroon,

Scientific Reports

2017

29

Studying Down syndrome recognition probabilities in Thai children with de‐identified computer‐aided facial analysis

Nattariya Vorravanpreecha, Thanayoot Lertboonnum, Rungrote Rodjanadit,

American Journal of Medical Genetics Part A

2018

29

Sex‐discordant monochorionic twins with blood and tissue chimerism

David Rodriguez‐Buritica, Kitiwan Rojnueangnit, Ludwine Messiaen,

American Journal of Medical Genetics Part A

2015

26

Quality of life and comprehensive health supervision for children with Down syndrome in Thailand

Kitiwan Rojnueangnit, Penrawee Khaosamlee, Issarapa Chunsuwan,

Journal of Community Genetics

2020

25

Clinical course, mutations and its functional characteristics of infantile-onset Pompe disease in Thailand

Lukana Ngiwsara, Duangrurdee Wattanasirichaigoon, Thipwimol Tim‐Aroon,

BMC Medical Genetics

2019

19

Expanding phenotypic and mutational spectra of mitochondrial HMG-CoA synthase deficiency

Kitiwan Rojnueangnit, Parisa Maneechai, Patcharapa Thaweekul,

European Journal of Medical Genetics

2020

18

Novel SOX10 Mutations in Waardenburg Syndrome: Functional Characterization and Genotype-Phenotype Analysis

Supranee Thongpradit, Natini Jinawath, Asif Javed,

Frontiers in Genetics

2020

18

Page 1